Shanghai Sanyou Medical Co, Ltd.
FDA 510(k) & PMA Approved Devices — 8 products
Total Devices8
Categories4
Latest Approval2023-12-12
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K230872 | Halis Lumbar Cage System, Lydia Anterior Lumbar Fusion System, Dica Direction Changeable Lumbar Cage System, KEYSTONE Cage System | MAX | 2023-12-12 | View |
| 510(k) | K230961 | Zeus Spinal System | NKB | 2023-10-10 | View |
| 510(k) | K231931 | Adena-Zina Spinal System | NKB | 2023-07-28 | View |
| 510(k) | K211689 | KEYSTONE PEEK Cage System | MAX | 2021-09-21 | View |
| 510(k) | K212066 | Adena-Zina System | NKB | 2021-08-16 | View |
| 510(k) | K163366 | Shanghai Sanyou CARMEN Cervical Fusion System | KWQ | 2017-10-05 | View |
| 510(k) | K163422 | Shanghai Sanyou PEEK Cage System | ODP | 2017-09-18 | View |
| 510(k) | K152781 | Adena-Zina System | NKB | 2016-02-12 | View |
No matching devices.